Atypical GH Insensitivity Syndrome and Severe Insulin-Like Growth Factor-I Deficiency Resulting from Compound Heterozygous Mutations of the GH Receptor, Including a Novel Frameshift Mutation Affecting the Intracellular Domain

2010 ◽  
Vol 74 (6) ◽  
pp. 406-411 ◽  
Author(s):  
Javier Aisenberg ◽  
Valerie Auyeung ◽  
Helio F. Pedro ◽  
Rachel Sugalski ◽  
Amy Chartoff ◽  
...  
Keyword(s):  
Growth Factor ◽  
Frameshift Mutation ◽  
Compound Heterozygous ◽  
Insulin Like Growth Factor ◽  
Intracellular Domain ◽  
Factor I ◽  
Gh Receptor ◽  
Growth Factor I ◽  
Compound Heterozygous Mutations

scholarly journals Growth Hormone (GH) Receptor Blockade with a PEG-Modified GH (B2036-PEG) Lowers Serum Insulin-Like Growth Factor-I but Does Not Acutely Stimulate Serum GH1

1999 ◽  
Vol 84 (6) ◽  
pp. 2098-2103 ◽  
Author(s):  
Michael O. Thorner ◽  
Christian J. Strasburger ◽  
Zida Wu ◽  
Martin Straume ◽  
Martin Bidlingmaier ◽  
...  
Keyword(s):  
Growth Hormone ◽  
Growth Factor ◽  
Serum Insulin ◽  
Receptor Blockade ◽  
Insulin Like Growth Factor ◽  
Factor I ◽  
Gh Receptor ◽  
Growth Factor I
Sign in / Sign up

Export Citation Format

Share Document